Taddei M - Search Results

1

Oxime amides as a novel zinc binding group in histone deacetylase inhibitors: synthesis, biological activity, and computational evaluation.

Botta CB, Cabri W, Cini E, De Cesare L, Fattorusso C, Giannini G, Persico M, Petrella A, Rondinelli F, Rodriquez M, Russo A, Taddei M. Botta CB, et al. Among authors: taddei m. J Med Chem. 2011 Apr 14;54(7):2165-82. doi: 10.1021/jm101373a. Epub 2011 Mar 18. J Med Chem. 2011. PMID: 21417297

2

Solid-phase synthesis of conformationally constrained peptidomimetics based on a 3,6-disubstituted-1,4-diazepan-2,5-dione core.

Lampariello LR, Piras D, Rodriquez M, Taddei M. Lampariello LR, et al. Among authors: taddei m. J Org Chem. 2003 Oct 3;68(20):7893-5. doi: 10.1021/jo034785d. J Org Chem. 2003. PMID: 14510574

3

Ionic liquid as a suitable phase for multistep parallel synthesis of an array of isoxazolines.

Rodriquez M, Sega A, Taddei M. Rodriquez M, et al. Among authors: taddei m. Org Lett. 2003 Oct 30;5(22):4029-31. doi: 10.1021/ol035399l. Org Lett. 2003. PMID: 14572241

4

Colorimetric tools for solid-phase organic synthesis.

Gaggini F, Porcheddu A, Reginato G, Rodriquez M, Taddei M. Gaggini F, et al. Among authors: taddei m. J Comb Chem. 2004 Sep-Oct;6(5):805-10. doi: 10.1021/cc049963a. J Comb Chem. 2004. PMID: 15360217

5

Total synthesis, NMR solution structure, and binding model of the potent histone deacetylase inhibitor FR235222.

Rodriquez M, Terracciano S, Cini E, Settembrini G, Bruno I, Bifulco G, Taddei M, Gomez-Paloma L. Rodriquez M, et al. Among authors: taddei m. Angew Chem Int Ed Engl. 2006 Jan 9;45(3):423-7. doi: 10.1002/anie.200501995. Angew Chem Int Ed Engl. 2006. PMID: 16311994 No abstract available.

6

Synthesis of 2-amino-8-oxodecanoic acids (Aodas) present in natural hystone deacetylase inhibitors.

Rodriquez M, Bruno I, Cini E, Marchetti M, Taddei M, Gomez-Paloma L. Rodriquez M, et al. Among authors: taddei m. J Org Chem. 2006 Jan 6;71(1):103-7. doi: 10.1021/jo0518250. J Org Chem. 2006. PMID: 16388624

7

Chemistry and biology of chromatin remodeling agents: state of art and future perspectives of HDAC inhibitors.

Rodriquez M, Aquino M, Bruno I, De Martino G, Taddei M, Gomez-Paloma L. Rodriquez M, et al. Among authors: taddei m. Curr Med Chem. 2006;13(10):1119-39. doi: 10.2174/092986706776360905. Curr Med Chem. 2006. PMID: 16719774 Review.

8

Design and synthesis of cyclopeptide analogues of the potent histone deacetylase inhibitor FR235222.

Gomez-Paloma L, Bruno I, Cini E, Khochbin S, Rodriquez M, Taddei M, Terracciano S, Sadoul K. Gomez-Paloma L, et al. Among authors: taddei m. ChemMedChem. 2007 Oct;2(10):1511-9. doi: 10.1002/cmdc.200700095. ChemMedChem. 2007. PMID: 17694590

9

Effects of FR235222, a novel HDAC inhibitor, in proliferation and apoptosis of human leukaemia cell lines: role of annexin A1.

Petrella A, D'Acunto CW, Rodriquez M, Festa M, Tosco A, Bruno I, Terracciano S, Taddei M, Paloma LG, Parente L. Petrella A, et al. Among authors: taddei m. Eur J Cancer. 2008 Mar;44(5):740-9. doi: 10.1016/j.ejca.2008.01.023. Epub 2008 Mar 4. Eur J Cancer. 2008. PMID: 18295477

10

Molecular modeling studies toward the structural optimization of new cyclopeptide-based HDAC inhibitors modeled on the natural product FR235222.

Di Micco S, Terracciano S, Bruno I, Rodriquez M, Riccio R, Taddei M, Bifulco G. Di Micco S, et al. Among authors: taddei m. Bioorg Med Chem. 2008 Sep 15;16(18):8635-42. doi: 10.1016/j.bmc.2008.08.003. Epub 2008 Aug 6. Bioorg Med Chem. 2008. PMID: 18715788

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